No photo of Ilse Paetau
  • PL 63 (Haartmaninkatu 8)

    00014

    Finland

20052018
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Keywords

  • 319 Forensic science and other medical sciences
  • 3112 Neurosciences
  • Mitochondrial disease

International and National Collaboration Publications and projects within past five years.

Publications 2005 2018

Loss of mtDNA activates astrocytes and leads to spongiotic encephalopathy

Ignatenko, O., Chilov, D., Paetau, I., de Miguel, E., Jackson, C. B., Capin, G., Paetau, A., Terzioglu, M., Euro, L. & Suomalainen, A., 4 Jan 2018, In : Nature Communications. 9, 12 p., 70.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

Mitochondrial DNA Replication Defects Disturb Cellular dNTP Pools and Remodel One-Carbon Metabolism

Nikkanen, J., Forsstrom, S., Euro, L., Paetau, I., Kohnz, R. A., Wang, L., Chilov, D., Viinamaki, J., Roivainen, A., Marjamaki, P., Liljenback, H., Ahola, S., Buzkova, J., Terzioglu, M., Khan, N. A., Pirnes-Karhu, S., Paetau, A., Lonnqvist, T., Sajantila, A., Isohanni, P. & 6 othersTyynismaa, H., Nomura, D. K., Battersby, B. J., Velagapudi, V., Carroll, C. J. & Suomalainen, A., 12 Apr 2016, In : Cell Metabolism. 23, 4, p. 635-648 14 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access

Effective treatment of mitochondrial myopathy by nicotinamide riboside, a vitamin B3

Khan, N. A., Auranen, M., Paetau, I., Pirinen, E., Euro, L., Forsström, S., Pasila, L., Velagapudi, V., Carroll, C. J., Auwerx, J. & Suomalainen, A., Jun 2014, In : EMBO molecular medicine. 6, 6, p. 721-731 11 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

POLG1 manifestations in childhood: A study of 136 children

Isohanni, P., Hakonen, A. H., Euro, L., Paetau, I., Linnankivi, T., Liukkonen, E., Wallden, T., Luostarinen, L., Valanne, L., Paetau, A., Uusimaa, J., Lönnqvist, T., Suomalainen, A. & Pihko, H., 2011, In : Neurology. 76, 9, p. 811-815 5 p.

Research output: Contribution to journalArticleScientificpeer-review

Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European origin

Hakonen, A. H., Heiskanen, S., Juvonen, V., Paetau, I., Luoma, P., Rantamäki, M., Van Goethem, G., Löfgren, A., Hackman, P., Paetau, A., Kaakkola, S., Majamaa, K., Varilo, T., Udd, B., Kääriäinen, H., Bindoff, L. A. & Suomalainen, A. E., 2005, In : American Journal of Human Genetics. 77, 3, p. 430-441 12 p.

Research output: Contribution to journalArticleScientificpeer-review